Category:Neurodegenerative disorders
From WikiMD's Wellness Encyclopedia
Subcategories
This category has the following 4 subcategories, out of 4 total.
C
D
M
T
Pages in category "Neurodegenerative disorders"
The following 185 pages are in this category, out of 185 total.
A
C
- CDD-0034
- CDD-0097
- CDD-0098
- Cell-based therapies for Parkinson's disease
- Cerebellar abiotrophy
- Ceroid lipofuscinois, neuronal 2, late infantile
- Ceroid lipofuscinois, neuronal 3, juvenile
- Ceroid lipofuscinois, neuronal 4, adult type
- Ceroid lipofuscinois, neuronal 5, late infantile
- Ceroid lipofuscinois, neuronal 6, late infantile
- CHMP2B
- CISD2
- Classic creutzfeldt-jakob disease
- CLCN6
- CLN3
- CLN6
- CLN8
- COA7
- COASY
- Cockayne syndrome type 2
- Corticobasal degeneration
- Creeping disease
- Creutzfeldt-Jakob disease
E
G
H
L
M
N
- N-sulfoglucosamine-3-sulfatase
- NDUFAF1
- NDUFAF8
- Necroptosis
- Neuroaxonal dystrophy, late infantile
- Neurodegeneration
- Neurodegenerative diseases
- Neurodegenerative Diseases
- Neurodegenerative disorder
- Neurodegenerative disorders
- Neuroferritinopathy
- Neurofibrillary tangles
- Neuromelanin
- Neuronal ceroid lipofuscinosis
- Neuronal loss
- Niemann-Pick disease type B
- Normal-pressure hydrocephalus
P
- Palmitoyl-protein thioesterase deficiency
- Paraoxonase
- PARK7
- Parkinson
- Parkinson disease
- Parkinson's Disease
- Parkinson's disease
- Parkinson’s disease
- Parthanatos
- PLA2G6
- Pontocerebellar hypoplasia
- Pontocerebellar hypoplasia type 1
- Pontocerebellar hypoplasia type 2
- Pontocerebellar hypoplasia type 3
- Pontocerebellar hypoplasia type 4
- Pontocerebellar hypoplasia type 5
- Pontocerebellar hypoplasia type 6
- PPP2R2B
- Primary progressive aphasia
- Prion
- Prion protein
- Prions
- Prosetin
- Protein aggregation
- Protein misfolding
- Protein misfolding cyclic amplification
- Proteinopathy
- PSP
- PYCR2
- Pyruvate dehydrogenase complex deficiency
S
- Semantic
- Semantic dementia
- Senile plaques
- Shy–Drager syndrome
- Slow virus
- SORL1
- Spastic ataxia Charlevoix-Saguenay type
- Spielmeyer-Vogt
- Spielmeyer–Vogt disease
- Ataxia with Oculomotor Apraxia Type 2
- Infantile onset spinocerebellar ataxia
- Spinocerebellar ataxia 28
- Spinocerebellar ataxia 34
- Spongiform encephalopathy
- Steele–Richardson–Olszewski syndrome, atypical
- Subacute sclerosing panencephalitis
- Synuclein
- Systemic atrophies primarily affecting the central nervous system
